A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239714



Internal ID20806754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77987246..78765455hg38UCSC Ensembl
chr15:78279588..79057797hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38778210
hg19778210
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579298
Supporting Variants
Samples
Known GenesACSBG1, ADAMTS7, CHRNA3, CHRNA5, CHRNB4, CIB2, CRABP1, DNAJA4, HYKK, IDH3A, IREB2, LOC646938, LOC91450, MIR5003, PSMA4, SH2D7, TBC1D2B, WDR61
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239714
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00131


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